Canonical Allele Identifier: CA808240851

Gene: GRM6

Linked Data

• dbSNP Id: rs1370136769
• MyVariant Identifiers: chr5:g.178422050_178422051del (hg19) ; chr5:g.178995049_178995050del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.178995051_178995052del , CM000667.2:g.178995051_178995052del	GRCh38
NC_000005.9:g.178422052_178422053del , CM000667.1:g.178422052_178422053del	GRCh37
NC_000005.8:g.178354658_178354659del	NCBI36
NG_008105.1:g.5074_5075del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517717.3:c.-16-90_-16-89del MANE Select	ENSP00000430767.1:n.-16-90_-16-89del
ENST00000650031.1:c.-16-90_-16-89del	ENSP00000497110.1:n.-16-90_-16-89del
ENST00000231188.9:c.-106_-105del	ENSP00000231188.5:n.-106_-105del
ENST00000517717.1:c.-16-90_-16-89del	ENSP00000430767.1:n.-16-90_-16-89del
NM_000843.3:c.-106_-105del	NP_000834.2:n.-106_-105del
NM_000843.4:c.-16-90_-16-89del MANE Select	NP_000834.2:n.-16-90_-16-89del